Dynamic changes of proteases and protease inhibitors revealed by microarray analysis in CA3 and entorhinal cortex during epileptogenesis in the rat

被引:52
作者
Gorter, Jan A.
Van Vliet, Erwin A.
Rauwerda, Han
Breit, Timo
Stad, Robert
van Schaik, Linda
Vreugdenhil, Erno
Redeker, Sandra
Hendriksen, Erik
Aronica, Eleonora
da Silva, Fernando H. Lopes
Wadman, Wytse J.
机构
[1] Univ Amsterdam, Gorter Swammerdam Inst Life Sci, Ctr Neurosci, NL-1098 SM Amsterdam, Netherlands
[2] Univ Amsterdam, Swammerdam Inst Life Sci, Micro Array Dept, Amsterdam, Netherlands
[3] Stichting Epilepsie Instellingen Nederland, Heemstede, Netherlands
[4] LACDR, Leiden, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Neuropathol, NL-1012 WX Amsterdam, Netherlands
关键词
cathepsins; caspases; calpain; matrix metalloproteinases; plasminogen activator; status epilepticus; epilepsy;
D O I
10.1111/j.1528-1167.2007.01290.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We investigated expression of genes involved in the proteolytic process during epileptogenesis in a rat model of temporal lobe epilepsy (TLE). In a previous microarray study we found prominent activation of this process, which reached highest expression during the acute and latent phase (1 week after SE) in CA3 and entorhinal cortex (EC). Detailed analysis shows differences in dynamics of the changes of several protease genes such as cathepsins, caspases, matrix metalloproteinases, and plasminogen activators. Most genes were acutely upregulated while others were mainly activated during the latent phase. Interestingly several proteolytic genes were still elevated in the chronic epileptic phase. Various protease inhibitors followed a similar time course. The identification of changes in the activation of genes involved in proteolysis at critical phases during epileptogenesis could point to potential time specific targets for intervention. The fact that several proteolytic genes were still activated in the chronic epileptic phase makes them interesting candidates to modify and slow down seizure progression.
引用
收藏
页码:53 / 64
页数:12
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